Allele Registry

Canonical Allele Identifier: PA339526

Gene: BRIP1 HGNC NCBI

ClinVar Allele:

213361

ClinVar RCV:

RCV000200748

RCV000408962

RCV000410527

RCV000567218

RCV003316114

ClinVar Variation:

216793

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Phe934Val	CA339524 NM_032043.3:c.2800T>G